Cell biology and genetics of minimal change disease [version 1; peer review: 2 approved]
Cell biology and genetics of minimal change disease [version 1; peer review: 2 approved]
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Publisher
England: Faculty of 1000 Ltd
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Language
English
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Publisher
England: Faculty of 1000 Ltd
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Contents
Minimal change disease (MCD) is an important cause of nephrotic syndrome and is characterized by massive proteinuria and hypoalbuminemia, resulting in edema and hypercholesterolemia. The podocyte plays a key role in filtration and its disruption results in a dramatic loss of function leading to proteinuria. Immunologic disturbance has been suggeste...
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Full title
Cell biology and genetics of minimal change disease [version 1; peer review: 2 approved]
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TN_cdi_doaj_primary_oai_doaj_org_article_7fbec73352a847b8b5b1247e27d428fc
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7fbec73352a847b8b5b1247e27d428fc
Other Identifiers
ISSN
2046-1402
E-ISSN
2046-1402
DOI
10.12688/f1000research.7300.1
